Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Carbon Disulfide | HCID 6348 | — |
| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 1-[1-(Thiophen-2-yl)cyclopentyl]methanamine | HCID 16495144 | — |
| Product | HCID 23348537 | HCID 23348537 | — |
Reaction Steps
A solution of 21.2 parts of sodium hydroxide in 500 parts of water is cooled to 10° C. and there is added successively 45.6 parts of carbon disulfide and then dropwise 95.83 parts of 1-(2-thienyl)-cyclopentanemethylamine (exothermic reaction). After the addition is complete, the whole is stirred for 30 minutes at room temperature. Then there are added 57.5 parts of ethyl chloroformate at 30° C. (exothermic reaction: cooling is necessary). The whole is stirred for 3 hours at 50° C. and further stirred overnight without heating. The product is extracted with benzene. The extract is dried, filtered and evaporated. The residue is poured onto 350 parts of water and the whole is heated for 3 hours at 80°-90° C. The mixture is cooled and the product is extracted with dichloromethane. The extract is dried, filtered and evaporated. The oily residue is distilled twice, yielding 88 parts of [1-(2-thienyl)cyclopentylmethyl]isothiocyanate; bp. 110° C. at 0.1 mm pressure; nD20 :1.5960; d2020 :1.1743.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04216217 |
|---|
| Source dataset | uspto-grants-1980_08 |
|---|
| ORD ID | ord-29421ad13992487a9747e93a86cf5509 |
|---|
| Source note | uspto-grants-1980_08 |
|---|